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Cancer Res. 2016 Nov 1;76(21):6146-6152. Epub 2016 Oct 11.

Metabolite and Microbiome Interplay in Cancer Immunotherapy.

Author information

1
Department of Environmental Health Sciences, Yale School of Public Health, Yale University, New Haven, Connecticut. siuzdak@scripps.edu caroline.johnson@yale.edu.
2
Pharmacokinetics, Dynamics and Metabolism, Pfizer Worldwide Research and Development, San Diego, California.
3
Department of Surgery, Scripps Clinic Medical Group, La Jolla, California.
4
Sanford Burnham Medical Research Institute, La Jolla, California.
5
Scripps Center for Metabolomics, The Scripps Research Institute, La Jolla, California. siuzdak@scripps.edu caroline.johnson@yale.edu.

Abstract

The role of the host microbiome has come to the forefront as a potential modulator of cancer metabolism and could be a future target for precision medicine. A recent study revealed that in colon cancer, bacteria form polysaccharide matrices called biofilms at a high frequency in the proximal colon. Comprehensive untargeted and stable isotope-assisted metabolomic analysis revealed that the bacteria utilize polyamine metabolites produced from colon adenomas/carcinomas to build these protective biofilms and may contribute to inflammation and proliferation observed in colon cancer. This study highlighted the importance of finding the biological origin of a metabolite and assessing its metabolism and mechanism of action. This led to a better understanding of host and microbial interactions, thereby aiding therapeutic design for cancer. In this review, we will discuss methodologies for identifying the biological origin and roles of metabolites in cancer progression and discuss the interactions of the microbiome and metabolites in immunity and cancer treatment, focusing on the flourishing field of cancer immunotherapy. Cancer Res; 76(21); 6146-52.

PMID:
27729325
PMCID:
PMC5093024
DOI:
10.1158/0008-5472.CAN-16-0309
[Indexed for MEDLINE]
Free PMC Article

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